Randomized Trial of Transcatheter Valve-in-Valve vs Redo Surgery for Bioprosthetic Mitral Dysfunction

Not Applicable

Recruiting

• Conditions: Mitral Prosthetic Valve Stenosis and Regurgitation
• Interventions: Procedure: Transcatheter Valve-in-Valve Intervention; Procedure: Redo Mitral valve surgery

• Registration Number: NCT04402931
• Lead Sponsor: Instituto Dante Pazzanese de Cardiologia

Brief Summary

Transcatheter valve-in-valve implantation has emerged as a valid alternative to redo surgery for patients with surgical bioprosthetic dysfunction. Nowadays, transcatheter, transeptal mitral valve-in-valve replacement (TsMViV) has been adopted in many centers worldwide. Some studies report low rates of periprocedural morbidity and mortality and favorable hemodynamic parameters of valve performance. However, medium and long-term data on TsMViV as compared to redo surgical mitral valve replacement (rSMVR) is not yet established. Studies of cost-effectiveness and cost-utility comparing both strategies were also not reported. In particular, late prosthesis durability and hemodynamic performance after TsMViV are largely unknown and need to be elucidated before widely indicated, especially among younger and low-risk surgical candidates with failed mitral bioprostheses.

Detailed Description

Prospective, randomized, controlled trial of transeptal, transcatheter mitral valve-in-valve versus redo surgical mitral valve replacement.

After multidisciplinary, heart team discussion, patients meeting inclusion criteria will be randomized 1:1 to receive either transcatheter, transeptal mitral valve-in-valve replacement (TsMViV) with the SAPIEN 3 transcatheter heart valve (THV) or redo, mitral valve replacement with 3 commercially available surgical bioprosthetic valves. A sub-randomization in the surgical group will define which bioprosthetic valve will be used. Patients will be seen for follow-up visits at discharge, 30 days, 6 months and annually through 10 years.

Study Timeline

• Study Start: 2020-02-17
• Status Verified: 2020-05
• Study First Submitted: 2020-05-09
• Study First Submitted QC: 2020-05-21
• Last Update Submitted: 2020-05-21
• Study First Posted: 2020-05-27
• Last Update Posted: 2020-05-27
• Primary Completion: 2023-12
• Study Completion: 2031-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

• Age<70 years;
• Symptoms of heart failure NYHA class>ll;
• Severe mitral bioprosthetic dysfunction (stenosis, regurgitation, mixed) defined by echocardiography;
• Heart team (including cardiac surgeon) agree on eligibility including assessment that transeptal, transcatheter mitral valve replacement (TsMVR) and redo surgical mitral valve replacement (rSMVR) are appropriate;
• The study patient or the study patient's legal representative informed of the nature of the study, agreed to its provisions and provided written informed consent as approved by the Institutional Review Board (IRB) center;
• The study patient agreed to comply with all required post- procedure follow-up visits including annual visits through 10 years and analysis close date visits, which was conducted as a phone follow-up;
• Heart team agreed (a priori) on treatment strategy for concomitant coronary disease (if present);
• Patient agreed to undergo redo surgical mitral valve replacement (rSMVR) if randomized to control treatment.

Exclusion Criteria

• Heart Team assessment of inoperability (including examining cardiac surgeon);
• Hostile chest;
• Evidence of an acute myocardial infarction < 1 month (30 days) before the intended treatment [defined as: Q wave Ml, or non-Q wave Ml with total creatine kinase (CK), creatine kinase MB isoform (CK-MB) and/or cardiac troponin elevations (WHO definition)];
• Concomitant severe valvular disease (aortic, tricuspid or pulmonic) requiring surgical intervention;
• Mitral mechanical prosthesis or mitral valve rings;
• Preexisting mechanical or bioprosthetic valve in other position with dysfunction;
• Complex coronary artery disease: unprotected left main coronary artery, Syntax score > 32 (in the absence of prior revascularization);
• Any therapeutic invasive cardiac procedure resulting in a permanent implant that is performed within 30 days of the index procedure (unless part of planned strategy for treatment of concomitant coronary artery disease). Implantation of a permanent pacemaker is not an exclusion criteria;
• Patients with planned concomitant surgical or transcatheter ablation for atrial fibrillation;
• Leukopenia (WBC < 3000 cell/mL), acute anemia (Hgb< 9 g/dL), thrombocytopenia (Pht< 50,000 cell/mL);
• Hypertrophic cardiomyopathy with or without obstruction (HOCM);
• Severe ventricular dysfunction with left-ventricular ejection fraction (LVEF) < 20%;
• Echocardiographic evidence of intracardiac mass, thrombus or vegetation;
• Active upper gastrointestinal (GI) bleeding within 3 months (90 days) prior to procedure;
• A known contraindication or hypersensitivity to all anticoagulation regimens, or inability to be anticoagulated for the study procedure;
• Clinically (by neurologist) or neuroimaging confirmed stroke or transient ischemic attack (TIA) within 3 months (90 days) of the procedure;
• Renal insufficiency (creatinine > 3.0 mg/dL) and/or renal replacement therapy at the time of screening;
• Estimated life expectancy < 24 months (730 days) due to carcinomas, chronic liver disease, chronic renal disease or chronic end stage pulmonary disease;
• Currently participating in an investigational drug or another device study;
• Active bacterial endocarditis within 6 months (180 days) of procedure;
• Patient refuses redo mitral valve replacement surgery.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Transcatheter Valve-in-Valve Intervention	Transcatheter Valve-in-Valve Intervention	Transcatheter Valve-in-Valve Intervention
Redo Surgery	Redo Mitral valve surgery	Surgical Mitral valve replacement

Primary Outcome Measures

Name	Time	Method
Rate of Major cardiovascular and Cerebrovascular events	12 months	All-cause death; Cardiovascular death; Disabling stroke (neurologist assessment)

Secondary Outcome Measures

Name	Time	Method
Rate of Procedure-related complications	30 days	Major vascular complications; * Bleeding and transfusions; * Atrial fibrillation; * Acute renal failure; * Left-ventricular outflow obstruction; * Reoperation
Rate of Rehospitalization	12 months	Rehospitalization at 12 months
Rate of Prosthetic Thrombosis	3 and 12 months	Prosthetic thrombosis at 3- and 12 months (as assessed by transesophageal echocardiography and multi-slice tomography).
Rate of Structural Valve dysfunction (as assessed by transthoracic echocardiography)	10 years	Structural valve dysfunction assessed annually, up to 10-year follow-up.
Rate of Bioprosthetic Valve Failure (as assessed by clinical outcomes and echocardiographic evaluations)	10 years	Bioprosthetic valve failure assessed annually, up to 10-year follow-up.

Trial Locations

Locations (1)

Instituto Dante Pazzanese de Cardiologia; 🇧🇷 São Paulo, Brazil